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44 Cards in this Set

  • Front
  • Back

Osteoporosis pathophys

age gender race lifestyle drugs


increase osteoclastic decrease osteoblastic


osteopenia decrease in BMD


changes in skeletal structure


increase risk fracture, hip, spine, wrist

osteoporosis cm

back pain


loss of height


stooped posture


easier to get bone fracture

Osteoporsis lab and dx

no definitive lab test


-biochemical markers sensitive to bone changes


BSAP, BMD, Bone density

osteoporosis medical interventions

drug therapy


ca 1200-12500


vit d 800-1000


estrogen and hormone therapy


biphosphonates, ibandronate

nursing intervention osteoporosis

-teach fr med adminsitration


-nutrition therapy: protein, mg, ca, vit k, vit d, trace minerals


-exercise


-stop smoking, home issues

Connective tissue disease

46 million people in US have at least one or more than 100 types of CT disease or arthritis


-arthritis: inflammation of one or more joints


inflam: RA and SLE


non: OA


systemic: gout

osteoarthritis pathophys

enzymes breakdown matrix and proteoglycans cannot manage fluid in joints


increase in cartilage loss and thinning


-cartilage erodes, joint space narrows, oestophytes develop, inflam response, enhanced deterioration


-subluxation deformities leading to TJR

nursing assesment arthrist

OA and RA may look similar


joint pain stiffness: intensifies post physical activity, decrease post rest


-skeletal muscle atrophy


-vertebral column changes


-joint changes: heberdens, bowchards nodes


-joint effusions: crepitus

arthritis labs and dx

xray: structural joint changes


MRI: vertebral or knee involvemnet

OA conservative pain management

pain: low and slow


1 tylenol, lidocaine


2 nsaids, cox2 opiods


3 joint injections


4 thermal therapy


5 diet


6 integrative therapies


7 physical therapy

OA surgical management arthroplasty

purpose: pain is no longer in control, loss of ADL, quality of life


-hips and knees most common


-total joint arthroplasty or replacement


contraindicated: infection, osteoporosis, rapidly progressive inflammation

arthroplast nursing medical pre op care

pain management


encourage autologous transfusions


collaborative consulations


assess for safety issues


hemodynamic and electrolyte status

arthroplasty post op care

neurovascular assesmnet 6P's


pain managemnt


anticoagulant


activity progression


continous passive motion: only knee

arthroplasty prevent infection

temo


wind: is this atelectasis or pneumonia


wound: look, no infection


water: UTI


walking


wonder drugs

arthroplasty complication: dislocation

abduction pillow (hip)


-do not sit or stand for a long time


do not cross legs over midline


do not cross ankles or kneea

arthroplasty complcaitcations: Hypotension

blood transfusions: POD 1/2


physiological cues


-strict intake and output


-OH alert

arthroplasty complications DVT prevention

compression stockings


anticoagulant therapy heparin (apTT), warfarin (PT), LMWH (Xa)


-unaffected side: active/passive ROM


-affected side: foot rotation and isometric exercises


-early ambulation

pulmonary embolism syndrome

chest pain


dyspnea


tachypnea


tachycardia


diaphoresis


anxiety

Fat embolism syndrome

petechial rash


RR insuff


cerebral involvment


minor: tachycardia, fever, retinal sings, jaundice, renal sings


lab: h/h low, thrombocytopenia, high ESR, fat macroglominemia

arthroplasty home interventions

rasied toilet seat


unobstructed walk areas


saftey rails in shower/bathroom


no scatter rugs: small carpet peieces don't stick to the floor

RA pathophys

-antibodies from attacking healthy tissue


-phagocutic activity, inflam response, inflam synovail membrane


-cartialge breakdown and panes formation


-fiborous and joint deformity


-fiborus tissue calcification


-local and systemic dysfunction

RA nursing assessment CM

inflammation bilateral and symmetrical


progress to other joints over years


affected joints painful and stuff


hard to move for 30 mins or after resting


activity decreases pain and stiffness

RA nursing assessment early stages

joint inflammation


systemic: low grade fever, fatigue, weakness, anorexia, parathesias

RA late joint CM

deformities


moderate to severe pain


morning stiffness

RA late systemic CM

osteoporosis


anemia


severe fatigue


weight loss


subQ nodules


vasculitis


organ dysfunctoins

Sjogren's syndrome

autoimmune destruction


associated with RA and fibromyalgia


sicca syndrome


xerostomia

Ra lab and dx

RF +


increased ANA titer


C3 and C4 decreased


CRP high


ESR high


CT/MRI/Xray/Arthrocentesis

Pharm tx RA

1st line: NSAIDS: asa, ibu, celecoxib


2nd line NSAID with disease modifying anti rheumatic drugs (DMARD) like methotrexate


glucocorticoids


biological response modifiers : neutralie tumor necrosis factor, etanercept, infliximad, adalimumab, abatacept

Methotrexate

3-6weeks


decrease B and T lymphocytes


SE: GI, hepatic fibrosis, bone marrow suppression

RA nursing management goals of therapy

decrease pain


increase mobility


comfort: rest, positioning, thermal therapy, supportive measures


reconstructive surgery

OA differenees

o65+


female 2:1


rf: aging, genetic factor


dx: degenerative


clinical signs: unilateral, WB joints, non systemic


activity: pain increased with activity


labs: ESR WNL


Drugs: NSAID, acet, analgesic therapy

RA differences

35-45


female 3:1


RF: autoimmune, emotional, envionrment


-inflammatory


-cm: bilateral, UE first, systemic


-activity decrease pain


-increase ESR


-drug: NSAID, methotrexate, cortico, BMADS

SLE pathophys

defective elimination of self reactive B cells


Increase in production of antibodies


damage to tissues or combine with antigens to form tissue damaging immune complexes


-chronic, progressive inflam CTD lead to major organ and system failure

SLE nursing assesment

physical: butterfly rash, polyarthrtitis, osteonecrosis, muscle atrophy, myaldgia


-psych


-organ failure


-kidney is biggest prob


-flare=recent sun


-transient lupus like s/s post procainamide

SLE lab and dx

+ ana titer


increased ESR


decreased C3 and C4


CBC: anemia, thrombocytopenia, leukocytosis, leukopenia


biopsy only absolute for dx

discoid lupus erythematuous nursing managment

only effects skin


dry raised scaly patches


dx: confirmed with biopsy


tx: topical cortisone and skin protection

SLE nursing managment

topical cortisone for face lesions


steriod therapy


immunosuppressive agents


avoid sun exposure


wear hat/clothes that shield skin


sun screen SPF 30


avoid crowns


alopecia is common: milk shampoos

Gout pathophys

Excessive uric acid from rate crystals deposited into joints and other tissues


-severe inflammation


-disease of kings and king of diseases

Primary gout

most common


-caused my inherited problem with purine metab


-uric acid production exceeds the kidneys ability to excrete


-increase blood levels


-25% family hx


-90% middle aged men

Secondary Gout

affects all ages and genders


hyperureecimia due to another health problem like renal problems, diuretic therapy, crash diets, chemotherapy

Gout nursing assesment

attack occurs fast 8-12 hours


PE: pain in joints


asymptomatic stage: unaware and no tx


acute gouty arthritis: pain and inflammation, great toe: podagra


chronic gout: deposits of rate crystal develop under skin and with/in major organs (renal)

Gout lab and dx

hyperuricemia


increased ESR and WBC


chronic gout: tophi: Na urate crystal deposits, renal calculi and stones

Gout TX

NSAIDS: indomethacin, naproxen


acute: colchicine, antiinflammatory agent, inhibits leukocyte infilatrion se GI


chronic xanthine oxidase inhibitors: allupurinal, febuxostat, probenecid, pegloticase

Gout nursing and medical tx

reduce pain


prevent complications


prevent future attacks


weight reduction


nutrition, diet management